ONTOLOGY REPORT - ANNOTATIONS


Term:hair disease
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Accession:DOID:421 term browser browse the term
Definition:Diseases affecting the orderly growth and persistence of hair.
Synonyms:exact_synonym: hair diseases
 primary_id: MESH:D006201;   RDO:0000413
For additional species annotation, visit the Alliance of Genome Resources.


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hair disease term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Eif2ak4 eukaryotic translation initiation factor 2 alpha kinase 4 JBrowse link NW_004936471 3,423,792 3,527,089 RGD:9068941
G Shoc2 SHOC2 leucine rich repeat scaffold protein JBrowse link NW_004936486 1,723,253 1,809,416 RGD:9068941
alopecia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcc2 ATP binding cassette subfamily C member 2 JBrowse link NW_004936636 292,631 341,999 RGD:9068941
G Ar androgen receptor JBrowse link NW_004936635 485,903 647,820 RGD:9068941
G Bdnf brain derived neurotrophic factor JBrowse link NW_004936540 5,530,081 5,582,765 RGD:9068941
G Brd4 bromodomain containing 4 JBrowse link NW_004936596 5,176,682 5,246,102 RGD:9068941
G Cdsn corneodesmosin JBrowse link NW_004936837 787,035 791,388 RGD:9068941
G Col7a1 collagen type VII alpha 1 chain JBrowse link NW_004936529 348,938 381,701 RGD:9068941
G Crh corticotropin releasing hormone JBrowse link NW_004936496 7,759,656 7,761,555 RGD:9068941
G Esr2 estrogen receptor 2 JBrowse link NW_004936495 7,956,168 8,018,356 RGD:9068941
G Far2 fatty acyl-CoA reductase 2 JBrowse link NW_004936760 1,265,803 1,406,405 RGD:9068941
G Foxn1 forkhead box N1 JBrowse link NW_004936538 4,717,509 4,745,504 RGD:9068941
G Hr HR lysine demethylase and nuclear receptor corepressor JBrowse link NW_004936555 5,936,431 5,954,852 RGD:9068941
G Igf1 insulin like growth factor 1 JBrowse link NW_004936492 11,709,623 11,784,028 RGD:9068941
G Mfn2 mitofusin 2 JBrowse link NW_004936474 767,754 795,258 RGD:9068941
G Mthfr methylenetetrahydrofolate reductase JBrowse link NW_004936474 623,438 637,849 RGD:9068941
G Parp1 poly(ADP-ribose) polymerase 1 JBrowse link NW_004936526 3,102,468 3,147,601 RGD:9068941
G Plcd1 phospholipase C delta 1 JBrowse link NW_004936473 27,364,404 27,387,337 RGD:9068941
G Srd5a2 steroid 5 alpha-reductase 2 JBrowse link NW_004936493 1,663,999 1,708,530 RGD:9068941
G Supv3l1 Suv3 like RNA helicase JBrowse link NW_004936521 9,237,081 9,264,441 RGD:9068941
G Tpmt thiopurine S-methyltransferase JBrowse link NW_004936552 3,899,445 3,917,774 RGD:9068941
G Vdr vitamin D receptor JBrowse link NW_004936512 5,741,836 5,800,999 RGD:9068941
G Zdhhc13 zinc finger DHHC-type containing 13 JBrowse link NW_004936654 220,391 267,383 RGD:9068941
G Zfp36 ZFP36 ring finger protein JBrowse link NW_004936661 2,251,148 2,253,527 RGD:9068941
alopecia areata term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ctla4 cytotoxic T-lymphocyte associated protein 4 JBrowse link NW_004936631 484,356 489,643 RGD:9068941
G Cxcl10 C-X-C motif chemokine ligand 10 JBrowse link NW_004936676 60,869 63,028 RGD:9068941
G Cxcl9 C-X-C motif chemokine ligand 9 JBrowse link NW_004936676 33,580 40,323 RGD:9068941
G Cxcr3 C-X-C motif chemokine receptor 3 JBrowse link NW_004936762 66,636 69,694 RGD:9068941
G Dnmt1 DNA methyltransferase 1 JBrowse link NW_004936659 520,181 565,496 RGD:9068941
G Ehmt2 euchromatic histone lysine methyltransferase 2 JBrowse link NW_004936727 1,648,451 1,663,294 RGD:9068941
G Hdac1 histone deacetylase 1 JBrowse link NW_004936474 15,320,635 15,351,418 RGD:9068941
G Hdac2 histone deacetylase 2 JBrowse link NW_004936679 2,448,676 2,474,641 RGD:9068941
G Hdac7 histone deacetylase 7 JBrowse link NW_004936512 5,680,564 5,701,182 RGD:9068941
G Ikzf4 IKAROS family zinc finger 4 JBrowse link NW_004936646 417,565 449,021 RGD:9068941
G Il18 interleukin 18 JBrowse link NW_004936612 2,306,963 2,325,086 RGD:9068941
G Il1rn interleukin 1 receptor antagonist JBrowse link NW_004936783 1,447,158 1,466,331 RGD:9068941
G Il2 interleukin 2 JBrowse link NW_004936662 1,594,953 1,599,625 RGD:9068941
G Il2ra interleukin 2 receptor subunit alpha JBrowse link NW_004936484 8,514,333 8,555,392 RGD:9068941
G Kdm1a lysine demethylase 1A JBrowse link NW_004936474 8,262,913 8,319,089 RGD:9068941
G Kdm4a lysine demethylase 4A JBrowse link NW_004936474 25,002,527 25,056,642 RGD:9068941
G Kdm4b lysine demethylase 4B JBrowse link NW_004936588 2,908,970 3,005,625 RGD:9068941
G Kdm4c lysine demethylase 4C JBrowse link NW_004936539 1,198,105 1,580,078 RGD:9068941
G Kdm5a lysine demethylase 5A JBrowse link NW_004936606 486,424 570,546 RGD:9068941
G Notch4 notch receptor 4 JBrowse link NW_004936727 1,386,842 1,409,823 RGD:9068941
G Prdx5 peroxiredoxin 5 JBrowse link NW_004936599 4,894,409 4,897,426 RGD:9068941
G Ptpn22 protein tyrosine phosphatase non-receptor type 22 JBrowse link NW_004936690 2,180,804 2,232,869 RGD:9068941
G Stx17 syntaxin 17 JBrowse link NW_004936524 8,324,562 8,381,244 RGD:9068941
G Trps1 transcriptional repressor GATA binding 1 JBrowse link NW_004936470 30,475,779 30,666,546 RGD:9068941
alopecia universalis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hr HR lysine demethylase and nuclear receptor corepressor JBrowse link NW_004936555 5,936,431 5,954,852 RGD:7240710
RGD:9068941
G Il4 interleukin 4 JBrowse link NW_004936647 2,510,457 2,518,576 RGD:9068941
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rbm28 RNA binding motif protein 28 JBrowse link NW_004936479 15,451,583 15,483,496 RGD:7240710
RGD:9068941
Alopecia-Mental Retardation Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ahsg alpha 2-HS glycoprotein JBrowse link NW_004936578 3,332,934 3,339,903 RGD:9068941
RGD:7240710
Amaurosis Hypertrichosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cnnm4 cyclin and CBS domain divalent metal cation transport mediator 4 JBrowse link NW_004936744 715,523 754,148 RGD:9068941
atrichia with papular lesions term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hr HR lysine demethylase and nuclear receptor corepressor JBrowse link NW_004936555 5,936,431 5,954,852 RGD:7240710
RGD:9068941
G Odc1 ornithine decarboxylase 1 JBrowse link NW_004936532 6,581,717 6,587,116 RGD:9068941
autosomal recessive congenital ichthyosis 11 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G St14 suppression of tumorigenicity 14 JBrowse link NW_004936572 2,137,820 2,182,674 RGD:7240710
RGD:9068941
Bamforth-Lazarus syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Bche butyrylcholinesterase JBrowse link NW_004936707 1,784,338 1,913,401 RGD:9068941
G Foxe1 forkhead box E1 JBrowse link NW_004936524 6,619,128 6,620,278 RGD:7240710
RGD:9068941
Barber-Say syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Twist2 twist family bHLH transcription factor 2 JBrowse link NW_004936745 2,067,272 2,067,948 RGD:7240710
RGD:9068941
Bjornstad syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC101961358 mitochondrial chaperone BCS1 JBrowse link NW_004936569 1,104,493 1,108,708 RGD:7240710
RGD:9068941
Brachycephaly, Trichomegaly, and Developmental Delay term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rps23 ribosomal protein S23 JBrowse link NW_004936469 1,523,667 1,525,830 RGD:9068941
RGD:7240710
Central Centrifugal Cicatricial Alopecia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Padi3 peptidyl arginine deiminase 3 JBrowse link NW_004936474 4,165,597 4,191,449 RGD:9068941
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Htra1 HtrA serine peptidase 1 JBrowse link NW_004936486 11,271,130 11,317,271 RGD:7240710
RGD:9068941
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dsg1 desmoglein 1 JBrowse link NW_004936682 1,854,637 1,889,426 RGD:7240710
RGD:9068941
congenital hypotrichosis with juvenile macular dystrophy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cdh3 cadherin 3 JBrowse link NW_004936475 18,908,031 18,954,402 RGD:7240710
RGD:9068941
Congenital Woolly Hair term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Liph lipase H JBrowse link NW_004936578 4,304,503 4,346,838 RGD:9068941
cortisone reductase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G H6pd hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase JBrowse link NW_004936623 3,359,624 3,376,598 RGD:9068941
G Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 JBrowse link NW_004936557 3,358,809 3,403,461 RGD:9068941
cortisone reductase deficiency 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G H6pd hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase JBrowse link NW_004936623 3,359,624 3,376,598 RGD:9068941
RGD:7240710
cortisone reductase deficiency 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hsd11b1 hydroxysteroid 11-beta dehydrogenase 1 JBrowse link NW_004936557 3,358,809 3,403,461 RGD:7240710
RGD:9068941
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ripk4 receptor interacting serine/threonine kinase 4 JBrowse link NW_004936500 2,017,519 2,038,777 RGD:9068941
Cutaneous Telangiectasia and Cancer Syndrome, Familial term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Atr ATR serine/threonine kinase JBrowse link NW_004936540 4,074,543 4,178,859 RGD:7240710
RGD:9068941
dilated cardiomyopathy with woolly hair and keratoderma term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dsp desmoplakin JBrowse link NW_004936534 5,029,008 5,076,467 RGD:7240710
RGD:9068941
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dsp desmoplakin JBrowse link NW_004936534 5,029,008 5,076,467 RGD:7240710
RGD:9068941
Ectodermal Dysplasia 4, Hair/Nail Type term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hoxc13 homeobox C13 JBrowse link NW_004936512 11,160,343 11,166,616 RGD:9068941
Ectodermal Dysplasia 9, Hair/Nail Type term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hoxc13 homeobox C13 JBrowse link NW_004936512 11,160,343 11,166,616 RGD:7240710
RGD:9068941
Eosinophilic Pustular Folliculitis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ccl26 C-C motif chemokine ligand 26 JBrowse link NW_004936543 2,414,948 2,416,922 RGD:9068941
Frontonasal Dysplasia 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Alx4 ALX homeobox 4 JBrowse link NW_004936562 4,316,550 4,326,022 RGD:7240710
RGD:9068941
Glomerulonephritis with Sparse Hair and Telangiectases term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sox18 SRY-box 18 JBrowse link NW_004936514 11,231,327 11,233,292 RGD:9068941
RGD:7240710
G Tcea2 transcription elongation factor A2 JBrowse link NW_004936514 11,243,021 11,251,216 RGD:9068941
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Antxr1 ANTXR cell adhesion molecule 1 JBrowse link NW_004936491 13,288,986 13,516,878 RGD:7240710
RGD:9068941
Hirsutism term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cacna1g calcium voltage-gated channel subunit alpha1 G JBrowse link NW_004936490 11,093,600 11,157,756 RGD:9068941
G Pomc proopiomelanocortin JBrowse link NW_004936493 7,060,747 7,065,276 RGD:9068941
G Smc1a structural maintenance of chromosomes 1A JBrowse link NW_004936751 332,351 388,756 RGD:9068941
hypertrichosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Arid1b AT-rich interaction domain 1B JBrowse link NW_004936489 8,811,094 9,202,423 RGD:9068941
G Asxl1 ASXL transcriptional regulator 1 JBrowse link NW_004936485 19,218,494 19,297,188 RGD:9068941
G Kcnj11 potassium voltage-gated channel subfamily J member 11 JBrowse link NW_004936528 1,685,015 1,688,220 RGD:9068941
G Naglu N-acetyl-alpha-glucosaminidase JBrowse link NW_004936490 17,305,033 17,312,167 RGD:9068941
G Slc29a3 solute carrier family 29 member 3 JBrowse link NW_004936521 7,417,914 7,452,695 RGD:9068941
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abca5 ATP binding cassette subfamily A member 5 JBrowse link NW_004936541 8,467,035 8,549,893 RGD:9068941
RGD:7240710
hypertrichotic osteochondrodysplasia Cantu type term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcc9 ATP binding cassette subfamily C member 9 JBrowse link NW_004936548 4,983,461 5,110,693 RGD:7240710
RGD:9068941
G Kcnj8 potassium voltage-gated channel subfamily J member 8 JBrowse link NW_004936548 5,125,583 5,132,490 RGD:9068941
G Muc3a mucin 3A, cell surface associated JBrowse link NW_004936543 886,333 904,504 RGD:9068941
hypotrichosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dsg4 desmoglein 4 JBrowse link NW_004936682 1,803,862 1,829,352 RGD:9068941
G Liph lipase H JBrowse link NW_004936578 4,304,503 4,346,838 RGD:9068941
G Lpar6 lysophosphatidic acid receptor 6 JBrowse link NW_004936565 1,688,218 1,689,876 RGD:7240710
RGD:9068941
G Rpl21 ribosomal protein L21 JBrowse link NW_004936472 22,523,470 22,538,299 RGD:9068941
G Snrpe small nuclear ribonucleoprotein polypeptide E JBrowse link NW_004936567 849,300 855,214 RGD:9068941
hypotrichosis 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Apcdd1 APC down-regulated 1 JBrowse link NW_004936626 1,217,240 1,237,741 RGD:7240710
RGD:9068941
G Lpar6 lysophosphatidic acid receptor 6 JBrowse link NW_004936565 1,688,218 1,689,876 RGD:9068941
G Snrpe small nuclear ribonucleoprotein polypeptide E JBrowse link NW_004936567 849,300 855,214 RGD:9068941
hypotrichosis 11 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Snrpe small nuclear ribonucleoprotein polypeptide E JBrowse link NW_004936567 849,300 855,214 RGD:7240710
RGD:9068941
hypotrichosis 12 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rpl21 ribosomal protein L21 JBrowse link NW_004936472 22,523,470 22,538,299 RGD:7240710
RGD:9068941
Hypotrichosis 14 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lss lanosterol synthase JBrowse link NW_004936778 323,120 351,100 RGD:9068941
RGD:7240710
hypotrichosis 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cdsn corneodesmosin JBrowse link NW_004936837 787,035 791,388 RGD:7240710
RGD:9068941
hypotrichosis 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hr HR lysine demethylase and nuclear receptor corepressor JBrowse link NW_004936555 5,936,431 5,954,852 RGD:7240710
RGD:9068941
hypotrichosis 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dsg4 desmoglein 4 JBrowse link NW_004936682 1,803,862 1,829,352 RGD:7240710
RGD:9068941
hypotrichosis 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Liph lipase H JBrowse link NW_004936578 4,304,503 4,346,838 RGD:7240710
RGD:9068941
hypotrichosis 8 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Krt25 keratin 25 JBrowse link NW_004936490 15,727,697 15,733,784 RGD:9068941
G Lpar6 lysophosphatidic acid receptor 6 JBrowse link NW_004936565 1,688,218 1,689,876 RGD:9068941
G Rb1 RB transcriptional corepressor 1 JBrowse link NW_004936565 1,596,227 1,746,706 RGD:9068941
hypotrichosis and recurrent skin vesicles term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC101956406 desmocollin-3 JBrowse link NW_004936682 2,126,394 2,161,672 RGD:7240710
RGD:9068941
Hypotrichosis-Lymphedema-Telangiectasia Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sox18 SRY-box 18 JBrowse link NW_004936514 11,231,327 11,233,292 RGD:7240710
RGD:9068941
G Tcea2 transcription elongation factor A2 JBrowse link NW_004936514 11,243,021 11,251,216 RGD:9068941
Ichthyosis Follicularis Atrichia Photophobia Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mbtps2 membrane bound transcription factor peptidase, site 2 JBrowse link NW_004936624 2,464,152 2,510,984 RGD:7240710
RGD:9068941
Loucks-Innes Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dph1 diphthamide biosynthesis 1 JBrowse link NW_004936538 8,100,977 8,110,704 RGD:9068941
RGD:7240710
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rin2 Ras and Rab interactor 2 JBrowse link NW_004936485 377,562 556,611 RGD:7240710
RGD:9068941
mandibulofacial dysostosis with alopecia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ednra endothelin receptor type A JBrowse link NW_004936535 1,950,117 2,005,786 RGD:7240710
RGD:9068941
Menkes disease term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Atp7a ATPase copper transporting alpha JBrowse link NW_004936683 2,874,022 2,936,214 RGD:7240710
RGD:9068941
G Cp ceruloplasmin JBrowse link NW_004936519 6,431,156 6,473,183 RGD:9068941
G Lox lysyl oxidase JBrowse link NW_004936575 2,526,067 2,533,996 RGD:9068941
Naxos Disease term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Jup junction plakoglobin JBrowse link NW_004936490 16,671,176 16,694,552 RGD:7240710
RGD:9068941
Nicolaides Baraitser Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Arid1b AT-rich interaction domain 1B JBrowse link NW_004936489 8,811,094 9,202,423 RGD:9068941
G Cdkl5 cyclin dependent kinase like 5 JBrowse link NW_004936844 101,815 271,254 RGD:9068941
G Rs1 retinoschisin 1 JBrowse link NW_004936844 284,938 314,524 RGD:9068941
G Smarca2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 JBrowse link NW_004936503 2,835,512 3,001,365 RGD:7240710
RGD:9068941
Nisch syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cldn1 claudin 1 JBrowse link NW_004936578 98,489 113,125 RGD:7240710
RGD:9068941
Noonan Syndrome-Like Disorder with Loose Anagen Hair term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Shoc2 SHOC2 leucine rich repeat scaffold protein JBrowse link NW_004936486 1,723,253 1,809,416 RGD:9068941
Noonan Syndrome-Like Disorder with Loose Anagen Hair 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Shoc2 SHOC2 leucine rich repeat scaffold protein JBrowse link NW_004936486 1,723,253 1,809,416 RGD:7240710
RGD:9068941
Noonan Syndrome-Like Disorder with Loose Anagen Hair 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ppp1cb protein phosphatase 1 catalytic subunit beta JBrowse link NW_004936493 3,981,364 4,002,083 RGD:9068941
RGD:7240710
Oliver-McFarlane Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pnpla6 patatin like phospholipase domain containing 6 JBrowse link NW_004936588 4,608,856 4,632,198 RGD:7240710
RGD:9068941
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kank2 KN motif and ankyrin repeat domains 2 JBrowse link NW_004936659 1,320,169 1,340,137 RGD:7240710
RGD:9068941
Photosensitive Trichothiodystrophy 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ercc2 ERCC excision repair 2, TFIIH core complex helicase subunit JBrowse link NW_004936706 1,816,561 1,829,638 RGD:7240710
RGD:9068941
G Gtf2h5 general transcription factor IIH subunit 5 JBrowse link NW_004936489 9,983,935 9,993,179 RGD:9068941
G Mplkip M-phase specific PLK1 interacting protein JBrowse link NW_004936478 15,421,612 15,423,894 RGD:9068941
Schopf-Schulz-Passarge Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Wnt10a Wnt family member 10A JBrowse link NW_004936569 1,309,140 1,321,923 RGD:7240710
RGD:9068941
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Poc1a POC1 centriolar protein A JBrowse link NW_004936529 3,423,588 3,495,698 RGD:7240710
RGD:9068941
Skin Fragility-Woolly Hair Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dsp desmoplakin JBrowse link NW_004936534 5,029,008 5,076,467 RGD:7240710
RGD:9068941
Spondyloepimetaphyseal Dysplasia, Genevieve Type term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nans N-acetylneuraminate synthase JBrowse link NW_004936524 6,772,831 6,791,854 RGD:9068941
RGD:7240710
G Trim14 tripartite motif containing 14 JBrowse link NW_004936524 6,797,788 6,816,582 RGD:9068941
T-cell immunodeficiency, congenital alopecia, and nail dystrophy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Foxn1 forkhead box N1 JBrowse link NW_004936538 4,717,509 4,745,504 RGD:7240710
RGD:9068941
Tricho-Dento-Osseous Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dlx3 distal-less homeobox 3 JBrowse link NW_004936490 11,625,862 11,630,035 RGD:7240710
RGD:9068941
Trichohepatoenteric Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nelfe negative elongation factor complex member E JBrowse link NW_004936727 1,589,942 1,596,009 RGD:9068941
G Skiv2l Ski2 like RNA helicase JBrowse link NW_004936727 1,579,208 1,590,215 RGD:9068941
G Ttc37 tetratricopeptide repeat domain 37 JBrowse link NW_004936523 7,786,629 7,885,220 RGD:9068941
Trichohepatoenteric Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Agk acylglycerol kinase JBrowse link NW_004936592 5,454,860 5,531,285 RGD:9068941
G Ttc37 tetratricopeptide repeat domain 37 JBrowse link NW_004936523 7,786,629 7,885,220 RGD:7240710
RGD:9068941
Trichohepatoenteric Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Skiv2l Ski2 like RNA helicase JBrowse link NW_004936727 1,579,208 1,590,215 RGD:7240710
RGD:9068941
Trichohepatoneurodevelopmental Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ccdc47 coiled-coil domain containing 47 JBrowse link NW_004936541 4,389,428 4,418,414 RGD:7240710
RGD:9068941
TRICHOMEGALY term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fgf5 fibroblast growth factor 5 JBrowse link NW_004936749 1,741,425 1,761,799 RGD:7240710
RGD:9068941
trichorhinophalangeal syndrome type I term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Aard alanine and arginine rich domain containing protein JBrowse link NW_004936470 29,320,937 29,325,193 RGD:9068941
G Acadl acyl-CoA dehydrogenase long chain JBrowse link NW_004936845 66,674 96,248 RGD:9068941
G Anxa13 annexin A13 JBrowse link NW_004936470 23,710,710 23,763,183 RGD:9068941
G Atad2 ATPase family AAA domain containing 2 JBrowse link NW_004936470 23,986,895 24,043,609 RGD:9068941
G Ccn3 cellular communication network factor 3 JBrowse link NW_004936470 27,178,439 27,185,554 RGD:9068941
G Col14a1 collagen type XIV alpha 1 chain JBrowse link NW_004936470 26,440,606 26,643,015 RGD:9068941
G Colec10 collectin subfamily member 10 JBrowse link NW_004936470 27,416,471 27,449,206 RGD:9068941
G Cps1 carbamoyl-phosphate synthase 1 JBrowse link NW_004936586 5,739,038 5,850,317 RGD:9068941
G CUNH8orf76 chromosome unknown C8orf76 homolog JBrowse link NW_004936470 24,093,346 24,110,514 RGD:9068941
G Deptor DEP domain containing MTOR interacting protein JBrowse link NW_004936470 26,698,707 26,837,470 RGD:9068941
G Derl1 derlin 1 JBrowse link NW_004936470 24,262,401 24,286,713 RGD:9068941
G Dscc1 DNA replication and sister chromatid cohesion 1 JBrowse link NW_004936470 26,849,541 26,869,040 RGD:9068941
G Eif3h eukaryotic translation initiation factor 3 subunit H JBrowse link NW_004936470 29,509,154 29,606,124 RGD:9068941
G Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 JBrowse link NW_004936470 26,994,549 27,099,758 RGD:9068941
G Erbb4 erb-b2 receptor tyrosine kinase 4 JBrowse link NW_004936586 4,065,767 5,100,690 RGD:9068941
G Ext1 exostosin glycosyltransferase 1 JBrowse link NW_004936470 28,303,213 28,566,470 RGD:9068941
G Fam83a family with sequence similarity 83 member A JBrowse link NW_004936470 24,119,688 24,138,413 RGD:9068941
G Fam91a1 family with sequence similarity 91 member A1 JBrowse link NW_004936470 23,645,233 23,684,841 RGD:9068941
G Fbxo32 F-box protein 32 JBrowse link NW_004936470 23,886,836 23,919,063 RGD:9068941
G Fer1l6 fer-1 like family member 6 JBrowse link NW_004936470 23,430,982 23,544,510 RGD:9068941
G Has2 hyaluronan synthase 2 JBrowse link NW_004936470 25,418,069 25,443,332 RGD:9068941
G Ikzf2 IKAROS family zinc finger 2 JBrowse link NW_004936586 3,522,614 3,676,070 RGD:9068941
G Kansl1l KAT8 regulatory NSL complex subunit 1 like JBrowse link NW_004936845 123,713 248,857 RGD:9068941
G Klhl38 kelch like family member 38 JBrowse link NW_004936470 23,786,950 23,796,422 RGD:9068941
G Lancl1 LanC like 1 JBrowse link NW_004936586 5,917,470 5,950,101 RGD:9068941
G LOC101966632 sperm-associated antigen 16 protein JBrowse link NW_004936586 3,264,953 3,407,823 RGD:9068941
G Lratd2 LRAT domain containing 2 JBrowse link NW_004936470 21,439,925 21,445,582 RGD:9068941
G Mal2 mal, T cell differentiation protein 2 JBrowse link NW_004936470 27,315,356 27,390,078 RGD:9068941
G Map2 microtubule associated protein 2 JBrowse link NW_004936845 475,406 752,600 RGD:9068941
G Med30 mediator complex subunit 30 JBrowse link NW_004936470 28,798,356 28,822,143 RGD:9068941
G Mrpl13 mitochondrial ribosomal protein L13 JBrowse link NW_004936470 26,386,511 26,424,480 RGD:9068941
G Mtbp MDM2 binding protein JBrowse link NW_004936470 26,312,670 26,386,410 RGD:9068941
G Mtss1 MTSS I-BAR domain containing 1 JBrowse link NW_004936470 22,963,498 23,117,923 RGD:9068941
G Myc MYC proto-oncogene, bHLH transcription factor JBrowse link NW_004936470 20,480,844 20,485,955 RGD:9068941
G Myl1 myosin light chain 1 JBrowse link NW_004936586 5,993,177 6,013,426 RGD:9068941
G Ndufb9 NADH:ubiquinone oxidoreductase subunit B9 JBrowse link NW_004936470 23,118,162 23,123,648 RGD:9068941
G Nsmce2 NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase JBrowse link NW_004936470 22,447,278 22,667,302 RGD:9068941
G Rad21 RAD21 cohesin complex component JBrowse link NW_004936470 29,377,793 29,403,422 RGD:9068941
G Rnf139 ring finger protein 139 JBrowse link NW_004936470 23,157,312 23,168,565 RGD:9068941
G Rpe ribulose-5-phosphate-3-epimerase JBrowse link NW_004936845 188,414 264,070 RGD:9068941
G Samd12 sterile alpha motif domain containing 12 JBrowse link NW_004936470 27,858,661 28,230,543 RGD:9068941
G Slc30a8 solute carrier family 30 member 8 JBrowse link NW_004936470 29,114,713 29,151,993 RGD:9068941
G Sntb1 syntrophin beta 1 JBrowse link NW_004936470 26,074,175 26,301,076 RGD:9068941
G Sqle squalene epoxidase JBrowse link NW_004936470 22,726,793 22,752,429 RGD:9068941
G Taf2 TATA-box binding protein associated factor 2 JBrowse link NW_004936470 26,871,865 26,951,804 RGD:9068941
G Tatdn1 TatD DNase domain containing 1 JBrowse link NW_004936470 23,123,693 23,156,764 RGD:9068941
G Tbc1d31 TBC1 domain family member 31 JBrowse link NW_004936470 24,164,666 24,236,091 RGD:9068941
G Tmem65 transmembrane protein 65 JBrowse link NW_004936470 23,247,722 23,284,894 RGD:9068941
G Tnfrsf11b TNF receptor superfamily member 11b JBrowse link NW_004936470 27,571,263 27,598,725 RGD:9068941
G Trib1 tribbles pseudokinase 1 JBrowse link NW_004936470 22,401,713 22,408,808 RGD:9068941
G Trmt12 tRNA methyltransferase 12 homolog JBrowse link NW_004936470 23,183,138 23,184,856 RGD:9068941
G Trps1 transcriptional repressor GATA binding 1 JBrowse link NW_004936470 30,475,779 30,666,546 RGD:7240710
RGD:9068941
G Unc80 unc-80 homolog, NALCN channel complex subunit JBrowse link NW_004936845 268,357 454,557 RGD:9068941
G Utp23 UTP23 small subunit processome component JBrowse link NW_004936470 29,489,354 29,495,171 RGD:9068941
G Washc5 WASH complex subunit 5 JBrowse link NW_004936470 22,667,354 22,725,538 RGD:9068941
G Wdyhv1 WDYHV motif containing 1 JBrowse link NW_004936470 23,957,498 23,974,834 RGD:9068941
G Zhx1 zinc fingers and homeoboxes 1 JBrowse link NW_004936470 24,058,718 24,084,535 RGD:9068941
G Zhx2 zinc fingers and homeoboxes 2 JBrowse link NW_004936470 24,315,371 24,476,063 RGD:9068941
G Znf572 zinc finger protein 572 JBrowse link NW_004936470 22,762,145 22,767,818 RGD:9068941
trichorhinophalangeal syndrome type III term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Trps1 transcriptional repressor GATA binding 1 JBrowse link NW_004936470 30,475,779 30,666,546 RGD:7240710
RGD:9068941
Uncombable Hair Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC101971622 trichohyalin JBrowse link NW_004936580 2,277,109 2,283,088 RGD:9068941
G Padi3 peptidyl arginine deiminase 3 JBrowse link NW_004936474 4,165,597 4,191,449 RGD:9068941
RGD:7240710
G Tgm3 transglutaminase 3 JBrowse link NW_004936485 16,259,197 16,325,167 RGD:9068941
Uncombable Hair Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tgm3 transglutaminase 3 JBrowse link NW_004936485 16,259,197 16,325,167 RGD:9068941
RGD:7240710
Uncombable Hair Syndrome 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC101971622 trichohyalin JBrowse link NW_004936580 2,277,109 2,283,088 RGD:7240710
RGD:9068941
Woodhouse Sakati Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dcaf17 DDB1 and CUL4 associated factor 17 JBrowse link NW_004936509 1,678,831 1,716,856 RGD:7240710
RGD:9068941
G Mettl8 methyltransferase like 8 JBrowse link NW_004936509 1,590,583 1,678,680 RGD:9068941
Woolly Hair, Autosomal Recessive term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Krt25 keratin 25 JBrowse link NW_004936490 15,727,697 15,733,784 RGD:9068941
G Lpar6 lysophosphatidic acid receptor 6 JBrowse link NW_004936565 1,688,218 1,689,876 RGD:9068941
G Rb1 RB transcriptional corepressor 1 JBrowse link NW_004936565 1,596,227 1,746,706 RGD:9068941
Woolly Hair, Autosomal Recessive 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Krt25 keratin 25 JBrowse link NW_004936490 15,727,697 15,733,784 RGD:9068941
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 10652
    disease of anatomical entity 10186
      integumentary system disease 1969
        hair disease 187
          Bamforth-Lazarus syndrome 2
          Bird Headed Dwarfism Montreal Type 0
          Bjornstad syndrome 1
          Brachycephaly, Trichomegaly, and Developmental Delay 1
          Catatrichy 0
          Congenital Woolly Hair + 3
          Copper Deficiency, Familial Benign 0
          Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome 1
          Dermoodontodysplasia 0
          Ectodermal Dysplasia 4, Hair/Nail Type 1
          Ectodermal Dysplasia 9, Hair/Nail Type 1
          FLOTCH Syndrome 0
          Hairy Palms and Soles 0
          Hirsutism + 8
          Kaler Garrity Stern Syndrome 0
          Katsantoni Papadakou Lagoyanni Syndrome 0
          Kozlowski-Krajewska Syndrome 0
          Martinez Monasterio Pinheiro Syndrome 0
          Menkes disease + 3
          Naxos Disease 1
          Oculotrichodysplasia 0
          Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 0
          Photosensitive Trichothiodystrophy 1 3
          Pili Annulati 0
          Pili Multigemini 0
          Pili Torti + 0
          Pseudofolliculitis Barbae 0
          Pseudomonilethrix 0
          Rodrigues Blindness 0
          Skin Fragility-Woolly Hair Syndrome 1
          TRICHOMEGALY 1
          Tricho-Dento-Osseous Syndrome 1
          Tricho-Dento-Osseous Syndrome 1 0
          Trichodysplasia-Xeroderma 0
          Trichohepatoenteric Syndrome + 4
          Trichohepatoneurodevelopmental Syndrome 1
          Trichostasis Spinulosa 0
          Uncombable Hair Syndrome + 3
          White Forelock with Malformations 0
          Woolly Hair, Autosomal Recessive + 3
          dilated cardiomyopathy with woolly hair and keratoderma + 1
          folliculitis + 1
          hypertrichosis + 12
          hypotrichosis + 85
          monilethrix + 0
          superficial mycosis + 0
          tinea capitis + 0
          trichorhinophalangeal syndrome type I 59
          trichorhinophalangeal syndrome type III 1
Path 2
Term Annotations click to browse term
  disease 10652
    disease of anatomical entity 10186
      nervous system disease 7878
        sensory system disease 3762
          skin disease 1969
            hair disease 187
              Bamforth-Lazarus syndrome 2
              Bird Headed Dwarfism Montreal Type 0
              Bjornstad syndrome 1
              Brachycephaly, Trichomegaly, and Developmental Delay 1
              Catatrichy 0
              Congenital Woolly Hair + 3
              Copper Deficiency, Familial Benign 0
              Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome 1
              Dermoodontodysplasia 0
              Ectodermal Dysplasia 4, Hair/Nail Type 1
              Ectodermal Dysplasia 9, Hair/Nail Type 1
              FLOTCH Syndrome 0
              Hairy Palms and Soles 0
              Hirsutism + 8
              Kaler Garrity Stern Syndrome 0
              Katsantoni Papadakou Lagoyanni Syndrome 0
              Kozlowski-Krajewska Syndrome 0
              Martinez Monasterio Pinheiro Syndrome 0
              Menkes disease + 3
              Naxos Disease 1
              Oculotrichodysplasia 0
              Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 0
              Photosensitive Trichothiodystrophy 1 3
              Pili Annulati 0
              Pili Multigemini 0
              Pili Torti + 0
              Pseudofolliculitis Barbae 0
              Pseudomonilethrix 0
              Rodrigues Blindness 0
              Skin Fragility-Woolly Hair Syndrome 1
              TRICHOMEGALY 1
              Tricho-Dento-Osseous Syndrome 1
              Tricho-Dento-Osseous Syndrome 1 0
              Trichodysplasia-Xeroderma 0
              Trichohepatoenteric Syndrome + 4
              Trichohepatoneurodevelopmental Syndrome 1
              Trichostasis Spinulosa 0
              Uncombable Hair Syndrome + 3
              White Forelock with Malformations 0
              Woolly Hair, Autosomal Recessive + 3
              dilated cardiomyopathy with woolly hair and keratoderma + 1
              folliculitis + 1
              hypertrichosis + 12
              hypotrichosis + 85
              monilethrix + 0
              superficial mycosis + 0
              tinea capitis + 0
              trichorhinophalangeal syndrome type I 59
              trichorhinophalangeal syndrome type III 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.